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Showing results (411-420 of 488) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 1998
Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneityA Fuchshuber, C C Deltas, S Berthold, et al.
Human Molecular Genetics|October 1, 1992
Mutations in the candidate gene for Norrie diseaseW Berger, D van de Pol, M Warburg, et al.
Clinical Lung Cancer|May 4, 2016
Lung Adenocarcinoma Staging Using the 2011 IASLC/ATS/ERS Classification: A Pooled Analysis of Adenocarcinoma In Situ and Minimally Invasive AdenocarcinomaMadhusmita Behera, Taofeek K Owonikoko, Anthony A Gal, et al.
Neurology|August 23, 2006
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27B A Neubauer, I Stefanova, C A Hübner, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
Annals of the New York Academy of Sciences|February 24, 2001
High frequency of mutations in four different disease genes in early-onset dementiaU Finckh, T Müller-Thomsen, U Mann, et al.
Ophthalmic Genetics|June 1, 1994
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyL I van den Born, M J van Schooneveld, L A de Jong, et al.
European Journal of Clinical Investigation|December 21, 2004
Fabry disease: overall effects of agalsidase alfa treatmentM Beck, R Ricci, U Widmer, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.
Pageof 49

Showing results (411-420 of 488) with videos related to

Sort By:
Pageof 49
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 1998
Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneityA Fuchshuber, C C Deltas, S Berthold, et al.
Human Molecular Genetics|October 1, 1992
Mutations in the candidate gene for Norrie diseaseW Berger, D van de Pol, M Warburg, et al.
Clinical Lung Cancer|May 4, 2016
Lung Adenocarcinoma Staging Using the 2011 IASLC/ATS/ERS Classification: A Pooled Analysis of Adenocarcinoma In Situ and Minimally Invasive AdenocarcinomaMadhusmita Behera, Taofeek K Owonikoko, Anthony A Gal, et al.
Neurology|August 23, 2006
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27B A Neubauer, I Stefanova, C A Hübner, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
Annals of the New York Academy of Sciences|February 24, 2001
High frequency of mutations in four different disease genes in early-onset dementiaU Finckh, T Müller-Thomsen, U Mann, et al.
Ophthalmic Genetics|June 1, 1994
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyL I van den Born, M J van Schooneveld, L A de Jong, et al.
European Journal of Clinical Investigation|December 21, 2004
Fabry disease: overall effects of agalsidase alfa treatmentM Beck, R Ricci, U Widmer, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.
Pageof 49